Aquaporin 1, Aquaporin 3 and Aquaporin 5 expression and EGFR mutation in malignant pleural mesotheliomas: an imunohistochemical and molecular study

被引:2
作者
Alabalik, Ulas [1 ]
Turkcu, Gul [1 ]
Keles, Ayse Nur [1 ]
Ibiloglu, Ibrahim [1 ]
Urakci, Zuhat [2 ]
Buyukbayram, Huseyin [1 ]
机构
[1] Dicle Univ, Sch Med, Dept Pathol, Diyarbakir, Turkey
[2] Dicle Univ, Sch Med, Dept Med Oncol, Diyarbakir, Turkey
关键词
Malignant pleural mesothelioma; aquaporin; EGFR; PCR; target treatment; SQUAMOUS-CELL CARCINOMA; LUNG-CANCER; WATER CHANNEL; COLORECTAL CARCINOGENESIS; GENE DISRUPTION; UP-REGULATION; PHASE-II; GROWTH; MIGRATION; GEFITINIB;
D O I
10.1080/13102818.2016.1264275
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Malignant pleural mesothelioma is a rare and fatal malignancy. This disease is, unfortunately, at its advanced stage when it is diagnosed. Survival time is usually not more than a few months. The aim of this study was to analyse the expression of Aquaporin 1, Aquaporin 3 and Aquaporin 5 in malignant pleural mesotheliomas and to explore the relationship of these levels of expression with epidermal growth factor receptor (EGFR) gene mutation and prognostic parameters. In this study, 60 cases diagnosed as malignant pleural mesothelioma among the pleural biopsy materials in the archives of the Pathology Department of Medical Faculty of Dicle University in 2003-2013 were evaluated. The tissues were stained immunohistochemically with antibodies against Aquaporin 1, Aquaporin 3 and Aquaporin 5, and the existence of EGFR mutation was investigated in the tissues by real-time polymerase chain reaction (PCR). The obtained results showed expression of Aquaporin 1, Aquaporin 3 and Aquaporin 5 in varied amounts in malignant pleural mesotheliomas. However, no significant relation was obtained thus far between the expression levels of these aquaporins and the prognostic parameters. No mutations were detected in the EGFR gene exons 18-21 by using real-time PCR. It could be suggested that although Aquaporin 1, Aquaporin 3 and Aquaporin 5 are expressed in malignant pleural mesothelioma, they do not have any effect on the prognostic parameters. Mutations in different domains of EGFR gene, other than exons 18-21, should be sought to develop new targeted treatments.
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收藏
页码:367 / 372
页数:6
相关论文
共 51 条
[1]   Receptor tyrosine kinase inhibitors and cytotoxic drugs affect pleural mesothelioma cell proliferation: insight into EGFR and ERK1/2 as antitumor targets [J].
Barbieri, Federica ;
Wuerth, Roberto ;
Favoni, Roberto E. ;
Pattarozzi, Alessandra ;
Gatti, Monica ;
Ratto, Alessandra ;
Ferrari, Angelo ;
Bajetto, Adriana ;
Florio, Tullio .
BIOCHEMICAL PHARMACOLOGY, 2011, 82 (10) :1467-1477
[2]   Identification of astrocytoma associated genes including cell surface markers [J].
Boon, K ;
Edwards, JB ;
Eberhart, CG ;
Riggins, GJ .
BMC CANCER, 2004, 4 (1)
[3]   Common EGFR mutations conferring sensitivity to gefitinib in lung adenocarcinoma are not prevalent in human malignant mesothelioma [J].
Cortese, JF ;
Gowda, AL ;
Wali, A ;
Eliason, JF ;
Pass, HI ;
Everson, RB .
INTERNATIONAL JOURNAL OF CANCER, 2006, 118 (02) :521-522
[4]   MALIGNANT PLEURAL MESOTHELIOMA AND EPIDERMAL GROWTH-FACTOR RECEPTOR (EGF-R) - RELATIONSHIP OF EGF-R WITH HISTOLOGY AND SURVIVAL USING FIXED PARAFFIN EMBEDDED TISSUE AND THE F4, MONOCLONAL-ANTIBODY [J].
DAZZI, H ;
HASLETON, PS ;
THATCHER, N ;
WILKES, S ;
SWINDELL, R ;
CHATTERJEE, AK .
BRITISH JOURNAL OF CANCER, 1990, 61 (06) :924-926
[5]   Epidermal growth factor receptor mutations in malignant pleural and peritoneal mesothelioma [J].
Enomoto, Yasunori ;
Kasai, Takahiko ;
Takeda, Maiko ;
Takano, Masato ;
Morita, Kohei ;
Kadota, Eiji ;
Iizuka, Norishige ;
Maruyama, Hiroshi ;
Haratake, Joji ;
Kojima, Yu ;
Ikeda, Naoya ;
Inatsugi, Naoki ;
Nonomura, Akitaka .
JOURNAL OF CLINICAL PATHOLOGY, 2012, 65 (06) :522-527
[6]   A comparison of epidermal growth factor receptor expression in malignant peritoneal and pleural mesothelioma [J].
Enomoto, Yasunori ;
Kasai, Takahiko ;
Takeda, Maiko ;
Takano, Masato ;
Morita, Kouhei ;
Kadota, Eiji ;
Iizuka, Norishige ;
Maruyama, Hiroshi ;
Haratake, Joji ;
Kojima, Yu ;
Ikeda, Naoya ;
Nonomura, Akitaka .
PATHOLOGY INTERNATIONAL, 2012, 62 (04) :226-231
[7]   The 2015 World Health Organization Classification of Tumors of the Pleura: Advances since the 2004 Classification [J].
Galateau-Salle, Francoise ;
Churg, Andrew ;
Roggli, Victor ;
Travis, William D. .
JOURNAL OF THORACIC ONCOLOGY, 2016, 11 (02) :142-154
[8]   Phase II study of erlotinib in patients with malignant pleural mesothelioma: A Southwest Oncology Group study [J].
Garland, Linda L. ;
Rankin, Cathryn ;
Gandara, David R. ;
Rivkin, Saul E. ;
Scott, Katherine M. ;
Nagle, Raymond B. ;
Klein-Szanto, Andres J. P. ;
Testa, Joseph R. ;
Altomare, Deborah A. ;
Borden, Ernest C. .
JOURNAL OF CLINICAL ONCOLOGY, 2007, 25 (17) :2406-2413
[9]   Gefitinib in patients with malignant mesothelioma: A phase II study by the cancer and leukemia group B [J].
Govindan, R ;
Kratzke, RA ;
Herndon, JE ;
Niehans, GA ;
Vollmer, R ;
Watson, D ;
Green, MR ;
Kindler, HL .
CLINICAL CANCER RESEARCH, 2005, 11 (06) :2300-2304
[10]   Prevention of skin tumorigenesis and impairment of epidermal cell proliferation by targeted aquaporin-3 gene disruption [J].
Hara-Chikuma, Mariko ;
Verkman, A. S. .
MOLECULAR AND CELLULAR BIOLOGY, 2008, 28 (01) :326-332